HappeningToo topic
Azathioprine reports
Browse community reports connected to Azathioprine. These reports can show that other people are describing similar experiences, but they do not prove that Azathioprine caused a symptom or reaction.
⚕️ Medicine safety note
Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.
30 problems
Abdominal Discomfort while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and abdominal discomfort appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and abdominal pain upper appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and abdominal pain appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and alopecia appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and anxiety appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and back pain appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and cough appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and decreased appetite appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and diarrhea appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and dizziness appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and fatigue appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and headache appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and hives appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and insomnia appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and itching appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and malaise appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and muscle spasms appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and muscular weakness appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and nausea appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and pain appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and peripheral swelling appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and rash appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and shortness of breath appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and skin redness appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and swelling appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and tingling or pins and needles appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and vomiting appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and weakness appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and weight decreased appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Azathioprine
FDA FAERS contains adverse-event reports in which Azathioprine and weight increased appear together. This does not establish that Azathioprine caused the reported reaction and cannot be used to estimate how often it occurs.
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